中国临床药理学杂志
中國臨床藥理學雜誌
중국림상약이학잡지
THE CHINESE JOURNAL OF CLINICAL PHARMACOLOGY
2014年
7期
617-619
,共3页
骆松梅%张秀华%徐艳艳%周岳娟
駱鬆梅%張秀華%徐豔豔%週嶽娟
락송매%장수화%서염염%주악연
二甲双胍%表阿霉素%肺腺癌%抑制%体内分布
二甲雙胍%錶阿黴素%肺腺癌%抑製%體內分佈
이갑쌍고%표아매소%폐선암%억제%체내분포
metformin%doxorubicin%lung adenocarcinoma%suppression%distribution in the body
目的:研究二甲双胍微泡对人肺腺癌裸鼠移植瘤抑制的影响。方法构建肺腺癌裸鼠皮下移植瘤模型,表阿霉素溶液组和联合二甲双胍微泡化疗药物组,每2 d尾静脉注射5 mg· kg-1药物。正常组和空白脂质微泡组,每2 d尾静脉注射0.9%NaCl和空白脂质微泡(均0.1 mL/20 g)。给药后,测量肿瘤体积变化;在不同时间点(0.5,2,4,8,12,24 h)取大鼠组织。测定载药体系对裸鼠皮下肺腺癌移植瘤的肿瘤抑制率,观察HE染色检测移植瘤及裸鼠各脏器的形态学特征的变化。结果对大鼠肿瘤抑制率,联合二甲双胍微泡化疗药物组与表阿霉素溶液组分别为(86.79±3.13)%,(67.55±3.61)%。表阿霉素在心脏的聚积量,联合二甲双胍微泡疗药物组显著低于表阿霉素溶液组( P<0.05)。结论二甲双胍微泡能促进盐酸表阿霉素抑制人肺腺癌A549细胞体外增殖,具有相对靶向性。
目的:研究二甲雙胍微泡對人肺腺癌裸鼠移植瘤抑製的影響。方法構建肺腺癌裸鼠皮下移植瘤模型,錶阿黴素溶液組和聯閤二甲雙胍微泡化療藥物組,每2 d尾靜脈註射5 mg· kg-1藥物。正常組和空白脂質微泡組,每2 d尾靜脈註射0.9%NaCl和空白脂質微泡(均0.1 mL/20 g)。給藥後,測量腫瘤體積變化;在不同時間點(0.5,2,4,8,12,24 h)取大鼠組織。測定載藥體繫對裸鼠皮下肺腺癌移植瘤的腫瘤抑製率,觀察HE染色檢測移植瘤及裸鼠各髒器的形態學特徵的變化。結果對大鼠腫瘤抑製率,聯閤二甲雙胍微泡化療藥物組與錶阿黴素溶液組分彆為(86.79±3.13)%,(67.55±3.61)%。錶阿黴素在心髒的聚積量,聯閤二甲雙胍微泡療藥物組顯著低于錶阿黴素溶液組( P<0.05)。結論二甲雙胍微泡能促進鹽痠錶阿黴素抑製人肺腺癌A549細胞體外增殖,具有相對靶嚮性。
목적:연구이갑쌍고미포대인폐선암라서이식류억제적영향。방법구건폐선암라서피하이식류모형,표아매소용액조화연합이갑쌍고미포화료약물조,매2 d미정맥주사5 mg· kg-1약물。정상조화공백지질미포조,매2 d미정맥주사0.9%NaCl화공백지질미포(균0.1 mL/20 g)。급약후,측량종류체적변화;재불동시간점(0.5,2,4,8,12,24 h)취대서조직。측정재약체계대라서피하폐선암이식류적종류억제솔,관찰HE염색검측이식류급라서각장기적형태학특정적변화。결과대대서종류억제솔,연합이갑쌍고미포화료약물조여표아매소용액조분별위(86.79±3.13)%,(67.55±3.61)%。표아매소재심장적취적량,연합이갑쌍고미포료약물조현저저우표아매소용액조( P<0.05)。결론이갑쌍고미포능촉진염산표아매소억제인폐선암A549세포체외증식,구유상대파향성。
Objective To investigate the inhibitory effect of metformin with lipid microbubbles on human lung adenocarcinoma in nude mice.Methods A model of lung adenocarcinoma xenograft in nude mice was established.Epirubicin group and epirubicin combined with metformin microbubble group ( ECMM) were intravenously injected into drugs at the dose of 5 mg · kg -1 every 2 d.Control group and blank microbubble group were intravenously injected into blank lipid microbubbles at the dose of 0.1 mL/20 g and 0.9%NaCl every 2 d.After treatment , tumor volume was detected.Tissues were obtained at the different time ( 0.5 , 2 , 4 , 8 , 12 , and 24 h ).The inhibition rate of drug carrier system on lung adenocarcinoma as well as morphological characteristics of HE stai-ning in the nude mice were detected.Results Tumor inhibition rates of epirubicin group and ECMM group were ( 67.55 ±3.61 )% and (86.79 ±3.13 )%, respectively.Accumulation of epirubicin in heart in ECMM group was significantly lower than that in epirubicin group ( P<0.05 ).Conclusion Combination with metformin microbubbles en-hances the inhibition of epirubicin on A 549 proliferation in vitro, indica-ting relative targeting.